Medtronic Cardiovascular Surgery-the Heart Valve Division: Medical Device Recalls in 2014

According to to data from the FDA, there were 2 medical device recalls made by Medtronic Cardiovascular Surgery-the Heart Valve Division in 2014. See the details of the recalls below.

You can see similar recalls for other firms.

• Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obturators are used with the Mosaic Porcine Aortic Bioprostheses.
• Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in conjunction with Hancock Conduit Model 105 to provide an alternate method for relief of left ventricular hypertension.